## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
β¦ LIBER β¦
Polymer supported diol functionalized ionic liquids: An efficient, heterogeneous and recyclable catalyst for 5-aryl-2-oxazolidinones synthesis from CO2 and aziridines under mild and solvent free condition
β Scribed by Rahul A. Watile; Dattatraya B. Bagal; Krishna M. Deshmukh; Kishor P. Dhake; Bhalchandra M. Bhanage
- Book ID
- 113803583
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 848 KB
- Volume
- 351
- Category
- Article
- ISSN
- 1381-1169
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
ChemInform Abstract: Zirconyl Chloride:
β
Ying Wu; Liang-Nian He; Ya Du; Jin-Quan Wang; Cheng-Xia Miao; Wei Li
π
Article
π
2009
π
John Wiley and Sons
β 39 KB
π 2 views
Lewis basic ionic liquids-catalyzed synt
β
Yang, Zhen-Zhen; He, Liang-Nian; Peng, Shi-Yong; Liu, An-Hua
π
Article
π
2010
π
Royal Society of Chemistry
π
English
β 303 KB
ChemInform Abstract: Lewis Basic Ionic L
β
Zhen-Zhen Yang; Liang-Nian He; Shi-Yong Peng; An-Hua Liu
π
Article
π
2011
π
John Wiley and Sons
β 36 KB
π 1 views
## Abstract Title agents like [C~4~DABCO]Br are able to catalyze the cycloaddition of carbon dioxide to aziridines (I) under solventβfree conditions without any additives.
Quaternary Ammonium Bromide Functionaliz
β
Du, Ya; Wu, Ying; Liu, An-Hua; He, Liang-Nian
π
Article
π
2008
π
American Chemical Society
π
English
β 131 KB
ChemInform Abstract: Quaternary Ammonium
β
Ya Du; Ying Wu; An-Hua Liu; Liang-Nian He
π
Article
π
2008
π
John Wiley and Sons
β 43 KB
Naturally occurring Ξ±-amino acid: a simp
β
Huan-Feng Jiang; Jin-Wu Ye; Chao-Rong Qi; Liang-Bin Huang
π
Article
π
2010
π
Elsevier Science
π
French
β 474 KB
Naturally occurring a-amino acid successfully catalyzed cycloaddition of aziridine with carbon dioxide to afford 5-aryl-2-oxazolisinones under mild conditions without the need of any additives. The scope of this reaction is very general, providing the corresponding products in good yields and excell